Dental/maxillofacial surgical procedure kit, non-medicated, reusable - UK MHRA Medical Device Registration

Dental/maxillofacial surgical procedure kit, non-medicated, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 96670. The device is manufactured by Aesculap AG from Germany, classified as General Medical Device. The authorized representative in the UK is B. Braun Medical Ltd.

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Dental/maxillofacial surgical procedure kit, non-medicated, reusable

MHRA Device ID: 96670•Ref: 96670

Device Type

General Medical Device

Devices

Dental/maxillofacial surgical procedure kit, non-medicated, reusable

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Sep 5, 2024

Manufacturer Information

Name

Aesculap AG

Address

Am Aesculap Platz

Tuttlingen, Germany

Created Date

Mar 26, 2021

Authorized Representative

Name

B. Braun Medical Ltd

Relationship Type

UK Responsible Person

Address

Brookdale Road Chapeltown

Sheffield, South Yorkshire, United Kingdom

Postcode: S35 2PW

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Other Products from Aesculap AG (10)

Other Products from Same Authorized Representative (10)

Dental/maxillofacial surgical procedure kit, non-medicated, reusable - UK MHRA Medical Device Registration

Device Type

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Type

Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

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